ClinVar Miner

Submissions for variant NM_001698.3(AUH):c.656-8C>T

gnomAD frequency: 0.00006  dbSNP: rs199879150
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002104443 SCV002431327 likely benign 3-methylglutaconic aciduria type 1 2021-07-28 criteria provided, single submitter clinical testing

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